TheoverarchingscientificobjectiveoftheCO-SCOREistoadvanceourunderstandingofhowgonadalaging affectsbioenergetics,abdominaladiposity,metabolism,anddiseaserisk,byconductingmechanistically-driven researchacrossthebasic-to-clinicaltranslationalspectrum.CO-SCOREProject2willleveragepreclinical modelsandinterventionstoprovideabi-directional,basic-to-clinicaltranslationalbridgebetweentheclinically relevantstudiesofProject1andthebasicdiscoverystudiesinProject3.Thelong-termobjectiveofProject2 istoworkcollaborativelywithCO-SCOREinvestigatorstodevelopbetterstrategiesfortreatingand preventingthepathologicalconsequencesofgonadalaging,whichdisproportionatelyafflictwomen. Menopauseisassociatedreducedlevelsofphysicalactivity,weightgain,andabdominaladiposity,and predisposeswomentoanumberofage-relateddisordersthatincludeinsulinresistance,diabetes,cancer, osteoporosis,andcardiovasculardisease.StudiesfromProjects1and2inthecurrentcycleoftheaward demonstratedthatestrogen(E2)isanimportantmediatorofthebioenergeticandmetabolicconsequencesof thelossofovarianfunction.Inourpreclinicalmodelofthelossofovarianfunction(surgicalovariectomy,OVX), wehavealsoobservedthatthedeclineinphysicalactivityoccursrapidly,precedeschangesinbodyweight andfatmass,andpredictsthesubsequentgaininweightandfatmass.StudiesfromProject3provide evidencethattheseOVX-inducedchangesinadiposetissuesaretheresultoftheinfiltrationandaccumulation ofbonemarrow-derivedadipocytes(BMDA),whichimpartaproinflammatoryharmfulphenotype.Recent evidencehassuggestedthatelevatedlevelsoffolliclestimulatinghormone(FSH)maycontributetoallofthese detrimentaleffectsthatoccurwiththelossofovarianfunction.
In AIM1 ofProject2,wemanipulatethese hormonesinapreclinicalmodeltodissecttheindependentandcombinedrolesof?E2and?FSHontheOVX- induceddeclineinspontaneousphysicalactivity(SPA),energybalance,theaccumulationofabdominalfat, andthefunctional,cellular,andmolecularcharacteristicsofadiposetissue.
In AIM2 ofProject2,weexamine themechanismsbywhichregularexercisecountersOVX-inducedchangesinthefunctional,cellularand molecularcharacteristicsofadiposetissue,includingtheenrichmentofBMDA.Thesestudieswillprovide novelevidenceregardingtherolesof?FSH,?SPA,andadiposetissueenrichmentofBMDAinthemetabolic consequencesofthelossofovarianfunction.Elucidatingthespecificcontributionsofthesefactorstothe detrimentalconsequencesofthelossofovarianfunctionwillleadtoinnovativestrategiesfortheprevention andtreatmentofage-relateddiseasesthataccompanyovarianfailure.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Specialized Center--Cooperative Agreements (U54)
Project #
9U54AG062319-06
Application #
9688832
Study Section
Special Emphasis Panel (ZRG1)
Project Start
Project End
Budget Start
2018-10-01
Budget End
2019-09-30
Support Year
6
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of Colorado Denver
Department
Type
DUNS #
041096314
City
Aurora
State
CO
Country
United States
Zip Code
80045